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. 2017 Aug 10;7:7833. doi: 10.1038/s41598-017-07947-6

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© The Author(s) 2017

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Exposure to hypoxia causes alterations in normalized position autocorrelation function (NPAF) in prostate cancer cells. (A) Normalized position autocorrelation function of beads fluctuations along with their exponential fit for shRb and shSCX LNCaP cells after 72 h of exposure to hypoxia or normoxia. (B) Relaxation time variation between different groups of cells (shRb, shSCX) after 72 h of hypoxia or normoxia. (C) Estimated viscosity from the measured relaxation time for different groups of cells (shRb, shSCX) after 72 h of hypoxia or normoxia. For A–C experiments were repeated 4 times (n = 4) and 10 cells were manipulated for each determination. Error bars represent ± S.D. *p < 0.05.